Complete trisomy 1q with mosaic Y;1 translocation: A recurrent aneuploidy presenting diagnostic dilemmas
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference20 articles.
1. Trisomy 13 mosaicism: study of serial cytogenetic changes in a case from early pregnancy to infancy
2. Trisomy 1 in a clinically recognized IVF pregnancy
3. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization
4. A common molecular basis for rearrangement disorders on chromosome 22q11
5. Prenatal diagnosis ofde novo trisomy 1(q21-qter)der(Y)t(Y;1) in a malformed live born
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1. A case of hidradenitis suppurativa linked to trisomy 1q;Journal of the European Academy of Dermatology and Venereology;2019-09-19
2. A rare case of de novo balanced reciprocal Y:1 chromosomal translocation in patient presenting with azoospermia;Andrologia;2019-02-03
3. Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns-like phenotype;Prenatal Diagnosis;2017-05-23
4. Involvement of interstitial telomeric sequences in two new cases of mosaicism for autosomal structural rearrangements;American Journal of Medical Genetics Part A;2014-11-26
5. Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: Molecular cytogenetic analysis, fetal pathology and review of the literature;Birth Defects Research Part A: Clinical and Molecular Teratology;2014-02-12
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